Package 59088-772-00

Brand: sumansetron

Generic: sumatriptan succinate, ondansetron
NDC Package

Package Facts

Identity

Package NDC 59088-772-00
Digits Only 5908877200
Product NDC 59088-772
Description

1 KIT in 1 PACKAGE (59088-772-00) * 9 BLISTER PACK in 1 CARTON (55111-292-09) / 9 TABLET in 1 BLISTER PACK * 30 TABLET, FILM COATED in 1 BOTTLE (45963-538-30)

Marketing

Marketing Status
Marketed Since 2021-01-01
Brand sumansetron
Generic sumatriptan succinate, ondansetron
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"spl_id": "f2054b5e-a881-1bd5-e053-2a95a90a015c", "openfda": {"rxcui": ["198052", "313161"], "spl_set_id": ["b69f0762-a2f7-28c7-e053-2995a90a0484"], "manufacturer_name": ["PureTek Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 PACKAGE (59088-772-00)  *  9 BLISTER PACK in 1 CARTON (55111-292-09)  / 9 TABLET in 1 BLISTER PACK *  30 TABLET, FILM COATED in 1 BOTTLE (45963-538-30)", "package_ndc": "59088-772-00", "marketing_start_date": "20210101"}], "brand_name": "Sumansetron", "product_id": "59088-772_f2054b5e-a881-1bd5-e053-2a95a90a015c", "dosage_form": "KIT", "product_ndc": "59088-772", "generic_name": "sumatriptan succinate, ondansetron", "labeler_name": "PureTek Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sumansetron", "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20210101", "listing_expiration_date": "20261231"}